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On the molecular nature of large-pore channels

Journal of molecular biology, 2021-08, Vol.433 (17), p.166994-166994, Article 166994

2021

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Carbenoxolone inhibits Pannexin1 channels through interactions in the first extracellular loop

The Journal of general physiology, 2016-02, Vol.147 (2), p.165-174

2016

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The P2X7 receptor forms a dye-permeable pore independent of its intracellular domain but dependent on membrane lipid composition

eLife, 2017-09, Vol.6

2017

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The Cryo-EM structure of pannexin 1 reveals unique motifs for ion selection and inhibition

eLife, 2020-02, Vol.9

2020

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Structure and assembly of calcium homeostasis modulator proteins

Nature structural & molecular biology, 2020-02, Vol.27 (2), p.150-159

2020

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Development and characterization of functional antibodies targeting NMDA receptors

Nature communications, 2022-02, Vol.13 (1), p.923-923, Article 923

2022

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A Drosophila protease cascade member, seminal metalloprotease-1, is activated stepwise by male factors and requires female factors for full activity

Genetics (Austin), 2014-04, Vol.196 (4), p.1117-1129

2014

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Mapping the putative G protein-coupled receptor (GPCR) docking site on GPCR kinase 2: insights from intact cell phosphorylation and recruitment assays

The Journal of biological chemistry, 2014-09, Vol.289 (36), p.25262-25275

2014

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Structure and function of GluN1-3A NMDA receptor excitatory glycine receptor channel

Science advances, 2024-04, Vol.10 (15), p.eadl5952-eadl5952

2024

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Subtle Modifications of the Pannexin-1 N-Terminus Results in Altered Channel Activity

Biophysical journal, 2018-02, Vol.114 (3), p.495a-495a

2018

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Searching for a Potential Voltage Sensor Intrinsic to Pannexin Channels

Biophysical journal, 2017-02, Vol.112 (3), p.550a-550a

2017

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Structural insights into binding of therapeutic channel blockers in NMDA receptors

Nature structural & molecular biology, 2022-06, Vol.29 (6), p.507-518

2022

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The weak voltage dependence of pannexin 1 channels can be tuned by N-terminal modifications

The Journal of general physiology, 2018-12, Vol.150 (12), p.1758-1768

2018

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Structural and functional mechanisms of anti-NMDAR autoimmune encephalitis

Nature structural & molecular biology, 2024-09

2024

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Expression, Purification, and Analysis of G-Protein-Coupled Receptor Kinases

Methods in Enzymology, 2013, Vol.521, p.347-366

2013

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Membrane Lipid Compositions Control Dye-Permeable Pore of the P2X7 Receptor

Biophysical journal, 2018-02, Vol.114 (3), p.126a-126a

2018

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Exploring the Three-Dimensional Architectures of Two Families of Large Pore Channels (CALHM1,2 and Pannexin1)

Biophysical journal, 2021-02, Vol.120 (3), p.211a-211a

2021

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Effective production of oligomeric membrane proteins by EarlyBac-insect cell system

Methods in enzymology, 2021, Vol.653, p.3

2021

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Publisher Correction: Structure and assembly of calcium homeostasis modulator proteins

Nature structural & molecular biology, 2020-03, Vol.27 (3), p.305-305

2020

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Mapping G Protein‐coupled Receptor (GPCR) Docking Site on GPCR Kinase 2: New Insights from Intact Cell Studies

The FASEB journal, 2015-04, Vol.29 (S1)

2015

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Mechanistic and Structural Studies of Pannexin Channels

Michalski, Kevin Ronald

2018

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Mapping the Putative G Protein-coupled Receptor (GPCR) Docking Site on GPCR Kinase 2

The Journal of biological chemistry, 2014-09, Vol.289 (36), p.25262-25275

2014

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Role of the GRK2 extreme amino terminus and active site tether in forming G protein‐coupled receptor docking site

The FASEB journal, 2013-04, Vol.27 (S1)

2013

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Predicting dose-volume histograms for organs-at-risk in IMRT planning

Medical physics (Lancaster), 2012-12, Vol.39 (12), p.7446-7461

2012

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Contemporary Update of a Multi-Institutional Predictive Nomogram for Salvage Radiotherapy After Radical Prostatectomy

Journal of clinical oncology, 2016-10, Vol.34 (30), p.3648-3654

2016

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On the molecular nature of large-pore channels

Carbenoxolone inhibits Pannexin1 channels through interactions in the first extracellular loop

The P2X7 receptor forms a dye-permeable pore independent of its intracellular domain but dependent on membrane lipid composition

The Cryo-EM structure of pannexin 1 reveals unique motifs for ion selection and inhibition

Structure and assembly of calcium homeostasis modulator proteins

Development and characterization of functional antibodies targeting NMDA receptors

A Drosophila protease cascade member, seminal metalloprotease-1, is activated stepwise by male factors and requires female factors for full activity

Mapping the putative G protein-coupled receptor (GPCR) docking site on GPCR kinase 2: insights from intact cell phosphorylation and recruitment assays

Structure and function of GluN1-3A NMDA receptor excitatory glycine receptor channel

Subtle Modifications of the Pannexin-1 N-Terminus Results in Altered Channel Activity

Searching for a Potential Voltage Sensor Intrinsic to Pannexin Channels

Structural insights into binding of therapeutic channel blockers in NMDA receptors

The weak voltage dependence of pannexin 1 channels can be tuned by N-terminal modifications

Structural and functional mechanisms of anti-NMDAR autoimmune encephalitis

Expression, Purification, and Analysis of G-Protein-Coupled Receptor Kinases

Membrane Lipid Compositions Control Dye-Permeable Pore of the P2X7 Receptor

Exploring the Three-Dimensional Architectures of Two Families of Large Pore Channels (CALHM1,2 and Pannexin1)

Effective production of oligomeric membrane proteins by EarlyBac-insect cell system

Publisher Correction: Structure and assembly of calcium homeostasis modulator proteins

Mapping G Protein‐coupled Receptor (GPCR) Docking Site on GPCR Kinase 2: New Insights from Intact Cell Studies

Mechanistic and Structural Studies of Pannexin Channels

Mapping the Putative G Protein-coupled Receptor (GPCR) Docking Site on GPCR Kinase 2

Role of the GRK2 extreme amino terminus and active site tether in forming G protein‐coupled receptor docking site

Predicting dose-volume histograms for organs-at-risk in IMRT planning

Contemporary Update of a Multi-Institutional Predictive Nomogram for Salvage Radiotherapy After Radical Prostatectomy

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